Tag | Content |
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EnhancerAtlas ID | HS105-21019 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:123430770-123432500 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr12:123432023-123432042 | CGGCACCACCTGGAGGCCG | - | 6.13 | EWSR1-FLI1 | MA0149.1 | chr12:123431763-123431781 | GGAAGGCCGGAAGCAAGG | + | 6.67 | RREB1 | MA0073.1 | chr12:123431574-123431594 | GCGGTGTGTGTGGTTTGTGG | - | 7.27 | TP53 | MA0106.3 | chr12:123431489-123431507 | AGCATGCACTGGCATGTC | - | 6.6 | TP53 | MA0106.3 | chr12:123431489-123431507 | AGCATGCACTGGCATGTC | + | 6.99 | ZNF263 | MA0528.1 | chr12:123432191-123432212 | GAAGCAGGAGGAGGGTGAGGT | + | 6.45 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I122942 | chr12 | 123426680 | 123432837 |
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Enhancer Sequence | TATGGACAGG AGGGGGACAA GAAGGAGAAG ACCCCAAAAC AGCCTCACTA TGTACTGGAG 60 CCCCCAGGCC TCTCTGGGTT TTTCCACCCT TCGCTGGCAC CAGCTATATG CAAGAGGTTC 120 CTAGGACAAA AAGACAAGAT CTAGCCCTTT CTCCCCCATC CCCTTCTGGC TCAATTTGAC 180 ACACTCAGGT AGTCAACTCC AGAGAGGCTC TTGGGGCAAT GGTTTCAGCT CCTGAAGGAT 240 AGGGCACGGT GCTGATCGTT AAGTCATCCC CAGTATTCAA AAGAGGCTAT TCATGACTGG 300 ACAGTTTTTG GTAATCCTTT CAGAAAAGGG GCCTCAACAC CTGACCCTGT GCTGGAAGAG 360 CAGGGGATGC CTTGGACGGT TGTTCAGGTT GTACACTATT TAAGAAACAC CAACTATTAA 420 AGGGGCACCA TTTACATCAT CAACATAAAT TATGTTAGAG CCTGAGGGTT GATAAAGAGA 480 TTCCAGAACT CCCAGCCAAG TTCTACATGG TGGCAGGGGC CATGGGTTGT GAAATCTGCC 540 CACACCATGT GCATGTCACC ACAGGCAGAG CTGAAAAGTG GTCCCAAGTG TGCGGCCATC 600 AGGCTGCTGT TCACCAGAGT CCTGGAAGAG GCCCCTGGGT GGAGCTGTTC ACACTTTGCA 660 GGAGTCACTA TGCTGATTCT CAAGCCAGCC AGGAAGGCTG CCTGAGAGTC CAGGACAGGA 720 GCATGCACTG GCATGTCCCA TGACCATGTG TCACGCCCCA GCCGCAGGAA GCATGCAGGG 780 TGCCTGAGTC ATGTTTGGCC ATGGGCGGTG TGTGTGGTTT GTGGAGATGA CTCGCTGGCT 840 ACACACAACA CATTCAGGCA TGGGGTGGAA AACCCAAACA GAGCCTTCCT GAGGCCTCCC 900 TTAGCTGAAC TAAAAGGCAG GGCCTGCAGT GCACACAGAG GTGGGGGCTG AGGGGGAGCT 960 CCAGGGTTTC TTGCTCCATC CCAGGGGCTG GTGGGAAGGC CGGAAGCAAG GGGTGGGGAG 1020 CAGCGTGCCA GAAATGGCTC AGACTCTAAA GAATAGATTT ACTTTCTCAT CTCAGTGAGG 1080 ACGGTGGGGA GGCTCGTGAC CAGGAACTTC GGGAAGAGGT CCTACCTGTG TGGCTGGAGA 1140 AGACTGTGGG GAGTGGCCTC ACCGGGGGCT GGGTGGGAGA TGGCTTCCTT TGCTACCCTG 1200 GTCTCAGGTC ACCAACACCA AAGGCTCCAA TGGAGCTGCG ACAATGACTT ACCCGGCACC 1260 ACCTGGAGGC CGTCATGCAT CCAAGCCCCT GCTCTAGAAG TACCCCACGT GGGCCTGGGT 1320 GACTGTGAGG GGGTTGCCTG TACCTGTCAC AGGGTCACAG CCCTGCCTGT CTGAACCCAG 1380 CCTGTCTGTC CCTTAGGGCT CGGGGGCACC CGCCCATTCA GGAAGCAGGA GGAGGGTGAG 1440 GTCAAACCTG GCTCACGGCC CTAGCTCGGA AGCAGAAGCA GTGCCGTGGG GTGGCCAGAG 1500 GGGACAGCAG CCTGCCCATG ATGGCATCAC AGCGGGCCCG CGATGGCATC ACAGCGGGCC 1560 CGCACCACCC CCACATACAC ACCAGGCACG TTCCAACCCA GGGCCTTTTC ACTGGCTGTG 1620 CCCTCTGCTC AGCACATACC TCCCAAGATG CCCGCCTCCT TCAGACCCTT ATTCAGATGT 1680 CCCCTTCTCA GCAAGACCTA TTTAACTTGT ATTTATTCAT TCATTTTAGA 1730
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